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  2. Medicines Act 1968 - Wikipedia

    en.wikipedia.org/wiki/Medicines_Act_1968

    Its official long title is "An Act to make new provision with respect to medicinal products and related matters, and for purposes connected therewith." [1] It governs the control of medicines for human use and for veterinary use, which includes the manufacture and supply of medicines, and the manufacture and supply of (medicated) animal feeding ...

  3. File:Medicines Act 1968 (UKPGA 1968-67).pdf - Wikipedia

    en.wikipedia.org/wiki/File:Medicines_Act_1968...

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Donate; Help; Learn to edit; Community portal; Recent changes; Upload file

  4. File:Medicines Act 1968 (UKPGA 1968-67 qp).pdf - Wikipedia

    en.wikipedia.org/wiki/File:Medicines_Act_1968...

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us

  5. Human Medicines Regulations 2012 - Wikipedia

    en.wikipedia.org/wiki/Human_Medicines...

    The Human Medicines Regulations 2012 in the United Kingdom were created, under statutory authority of the European Communities Act 1972 and the Medicines Act 1968 in 2012. The body responsible for their upkeep is the Medicines and Healthcare products Regulatory Agency. The regulations partially repealed the Medicines Act 1968 in line with EU ...

  6. Medicines and Healthcare products Regulatory Agency - Wikipedia

    en.wikipedia.org/wiki/Medicines_and_Healthcare...

    In 1999, the Medicines Control Agency (MCA) took over control of the General Practice Research Database (GPRD) from the Office for National Statistics. The Medicines Control Agency (MCA) and the Medical Devices Agency (MDA) merged in 2003 to form MHRA. In April 2012, the GPRD was rebranded as the Clinical Practice Research Datalink (CPRD).

  7. Commission on Human Medicines - Wikipedia

    en.wikipedia.org/wiki/Commission_on_Human_Medicines

    The Medicines and Healthcare products Regulatory Agency undertook a public consultation on proposals to amend the advisory body structure laid down in the Medicines Act 1968 in February 2005. Ministers agreed to a new structure with the establishment of the Commission that amalgamated the responsibilities of the Medicines Commission and the ...

  8. Committee on Safety of Medicines - Wikipedia

    en.wikipedia.org/wiki/Committee_on_Safety_of...

    The Committee on Safety of Medicines (CSM) was an independent advisory committee that advised the UK Licensing Authority on the quality, efficacy, and safety of medicines. Following the thalidomide tragedy of 1957 to 1961, in 1963 the government asked Sir Derrick Dunlop to set up a committee to investigate the control and introduction of new ...

  9. British Pharmacopoeia - Wikipedia

    en.wikipedia.org/wiki/British_Pharmacopoeia

    British Approved Names (BANs) are devised or selected by the British Pharmacopoeia Commission (BPC), and published by the Health Ministers, on the recommendation of the Commission on Human Medicines, to provide a list of names of substances or articles referred to in Section 100 of the Medicines Act 1968. BANs are short, distinctive names for ...